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        <rdf:type rdf:resource="http://www.w3.org/2002/07/owl#TransitiveProperty"/>
        <rdfs:label>has material basis in germline mutation in</rdfs:label>
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    <!-- http://identifiers.org/hgnc/23399 -->

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        <rdfs:label>FREM1</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0000110 -->

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        <rdfs:label>bifid nose</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0002254 -->

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        <rdfs:label>syndromic disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0012165 -->

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        <rdfs:label>BNAR syndrome</rdfs:label>
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        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6878</ns4:IAO_0000233>
        <ns5:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/bifid_nose_with_or_without_anorectal_and_renal_anomalies</ns5:curated_content_resource>
        <oboInOwl:hasExactSynonym>bifid nose with or without anorectal and renal anomalies</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:C567672</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:413305</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>BNAR syndrome is a very rare multiple congenital anomaly syndrome characterized by a bifid nose (with bulbous nasal tip but not associated with hypertelorism) with or without the presence of anal defects (i.e. anteriorly placed anus, rectal stenosis or atresia) and renal dysplasia (unilateral or bilateral renal agenesis) and without intellectual disability. BNAR syndrome is phenotypically related to Fraser syndrome and oculotrichoanal syndrome.</ns4:IAO_0000115>
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        <oboInOwl:hasDbXref>Orphanet:217266</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>SCTID:717940006</oboInOwl:hasDbXref>
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